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Q 7 Good Manufacturing Practice for Active Pharmaceutical ...

Q 7 Good Manufacturing Practice for Active Pharmaceutical ...

www.ema.europa.eu

applies to the manufacture of sterile APIs only up to the point immediately prior to the APIs being rendered sterile. The sterilization and aseptic processing of sterile APIs are not covered by this guidance, but should be performed in accordance with GMP guidelines for drug (medicinal) products as defined by local authorities.

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